CREAMOL HAND SANITIZER WIPE- alcohol swab
LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

CREAMOL HAND SANITIZING WIPE

Ethanol alcohol 80%. (w/w) Purpose: Antimicrobial

Antiseptic, Hand Sanitizer

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Wipe hands; discard.

For external use only. Flammable. Keep away from heat or flame

Do not use,

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wipe hands and dischard.

Other information

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

glycerin, Hypericum perforatum, Melaleuca alternifolia, water, parfum

NDC: 77892-0009-1 inner NDC: 77892-0009-1 outer

CREAMOL HAND SANITIZER WIPE
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:77892-0009
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
GLYCERIN (UNII: PDC6A3C0OX)
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:77892-0009-1	4 g in 1 POUCH; Type 0: Not a Combination Product	09/07/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	09/03/2020

Labeler - LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN (502952094)

Name	Address	ID/FEI	Business Operations
Establishment
LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN		502952094	manufacture(77892-0009)